Literature DB >> 6131456

Structure and biosynthesis of histocompatibility antigens (H-2, HLA).

B Dobberstein, S Kvist, L Roberts.   

Abstract

Histocompatibility antigens (H-2K, D and L, and HLA-A, B and C) are highly polymorphic cell surface proteins. Their primary structure has been determined by sequencing the protein, complementary DNAs (cDNAs) or genes in several laboratories. H-2Ld and Kd antigens are encoded by eight separate exons: one encodes the signal sequence, three encode the external domains, one encodes the membrane spanning segment and three encode the cytoplasmic domain. A similar structural organization has been found for an HLA gene. H-2 and HLA antigens are synthesized on membrane-bound ribosomes and are co-translationally inserted into the membrane of the endoplasmic reticulum. Here they assemble with beta 2-microglobulin, a small secretory protein. We describe the structure, the membrane insertion in vitro and in vivo, the intracellular transport and the surface expression of these antigens.

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Year:  1982        PMID: 6131456     DOI: 10.1098/rstb.1982.0163

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  2 in total

1.  Three-dimensional structure of beta 2-microglobulin.

Authors:  J W Becker; G N Reeke
Journal:  Proc Natl Acad Sci U S A       Date:  1985-06       Impact factor: 11.205

2.  Structural requirements for membrane assembly of proteins spanning the membrane several times.

Authors:  J Lipp; N Flint; M T Haeuptle; B Dobberstein
Journal:  J Cell Biol       Date:  1989-11       Impact factor: 10.539

  2 in total

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